FDA UDI Not in Commercial Distribution 🇺🇸 United States

Coral

DI: 10381780010982 · Model: 10-11-8585 · INTEGRA LIFESCIENCES CORPORATION
Product Codes
5
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Coral
Primary DI
10381780010982
Version / Model
10-11-8585
Catalog Number
10-11-8585
Company Name
INTEGRA LIFESCIENCES CORPORATION
Labeler DUNS
963856096
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-18
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
2d6a4f05-0c0a-4936-aff9-56494bc62e18
Distribution End Date
2015-11-15

Device Description

Non Self Tapping Fixed Screw 8.50mm x 85mm

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
KWP Appliance, Fixation, Spinal Interlaminal
KWQ Appliance, Fixation, Spinal Intervertebral Body
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Secondary M248101185851
Primary 10381780010982

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 8.50mm x 85mm